Diazepam Rectal Gel recall: Labeling Error
Diazepam Rectal Gel, 2.5 mg, TWIN PACK that Contains two pre-filled, unit-dose, rectal delivery systems with lubricating jelly and instructions for…
Why was Diazepam Rectal Gel recalled?
Labeling: Incorrect or Missing Lot and/or Exp Date: Product distributed without a lot number or expiration date on the outer carton.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot #: NBBN, Exp 02/22
- Product
- Diazepam Rectal Gel, 2.5 mg, TWIN PACK that Contains two pre-filled, unit-dose, rectal delivery systems with lubricating jelly and instructions for…
- Recalling firm
- Valeant Pharmaceuticals North America LLC
- Quantity
- 306 cartons
- Distribution
- Nationwide in the USA
- Recall date
- August 15, 2018
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)